Lead all QA functions as per cGMP / ICH Q7 Oversee QMS – Deviations, CAPA, OOS, Change Control Approve MBR, SOPs, validation & qualification documents Handle regulatory audits – USFDA, WHO, MHRA, etc. Review batch records & release API batches…
Receive, inspect, and verify incoming pharmaceutical materials and products. Ensure proper storage conditions as per GMP/GDP, including temperature controlled items. Maintain accurate inventory records using ERP/WMS systems. Perform FIFO/FEFO stock rotation to avoid expiry issues. Prepare and dispatch customer orders…